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Which of the following ethical guidelines describes a prospective participant's freedom to participate or not participate in a research study?


A) Promoting Justice
B) Promoting Health and Well-Being
C) Maintaining Privacy and Confidentiality
D) Promoting and Respecting Informed Decision Making

Correct Answer

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A person gives consent to participate in a study,is assigned to an intervention group,and is expected to remain in the study for 1 year.Which ethical principle is violated if after 6 months the participants in the treatment group have more problems than do the control participants but the researcher does not allow the members of the treatment group to stop the treatment?


A) Promoting Justice
B) Promoting Health and Well-Being
C) Maintaining Privacy and Confidentiality
D) Preserving Dignity

Correct Answer

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The Research Ethics Board (REB) is responsible for


A) approval of the research design.
B) protecting participants from undue risk.
C) ensuring that informed consent is obtained.
D) promotion of nursing research in health care institutions.

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A representative from a pharmaceutical company presents to the nurses at a long-term care facility a new product,a premedicated wound dressing,for treating pressure ulcers.The representative asks the nurses to try the new product for 1 month and compare its effectiveness with that of their current method of treatment.What type of unethical action does this situation demonstrate?


A) Intent to harm
B) Fraudulent behaviour
C) Scientific misconduct
D) Unauthorized research

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A patient newly diagnosed with breast cancer is asked to participate in a clinical trial for a new chemotherapy agent.This patient's freedom to participate or not participate in the study exercises protection of which of her human rights?


A) Right to fair treatment
B) Right to self-determination
C) Right to privacy and confidentiality
D) Right to anonymity

Correct Answer

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What is the basic human right that is violated when a researcher allows an unauthorized person access to study data containing information about participant identities and responses?


A) Justice
B) Beneficence
C) Confidentiality
D) Respect for persons

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The nurse researcher is planning a research study that will use human participants and their choice to participate in a specific treatment.The ethical principle that describes a prospective participant's freedom to choose whether or not to participate in the research study is what?


A) Justice
B) Beneficence
C) Confidentiality
D) Respect for persons

Correct Answer

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Which statements are accurate regarding the assent process for pediatric research?


A) A parental signature is required for a child to participate in a study.
B) The study protocol is reviewed with the parent and not the child.
C) The child should be able to express a preference for participation.
D) A child older than age 16 does not require a parent's signature for consent.
E) The child should understand the purpose of the study.

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A,C,E

The nurse researcher is planning a research study that will use human participants and their choice to participate in a specific treatment.The ethical principle that describes a prospective participant's freedom to choose whether or not to participate in the research study is what?


A) Promoting Justice
B) Promoting Health and Well-Being
C) Maintaining Privacy and Confidentiality
D) Preserving Dignity

Correct Answer

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What basic human right exists when participants have the right to withdraw from a study without penalty?


A) Right to self-determination
B) Right to anonymity and confidentiality
C) Right to fair treatment
D) Right to protection from discomfort and harm

Correct Answer

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How should a completed and signed informed consent form be handled?


A) It is turned over to the agency's REB for safekeeping.
B) It is sent to the Canadian Institutes of Health Research as evidence of compliance.
C) It is copied; one copy is given to the participant and the other is filed by the researcher in a secured location.
D) There is not special procedure for handling a consent form.

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D

The issue of personal privacy may be more difficult for nurse researchers to protect in qualitative studies than it is in quantitative studies for which reason?


A) Participants may be related to each other.
B) The researcher meets participants face to face in such studies.
C) Participants are not asked to sign an informed consent statement.
D) Verbatim quotations from participants may reveal personal information.

Correct Answer

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A mother agreed to let her young son participate in a research study because she believed that if she did not agree,her child would be denied drug therapy.What right has been violated in this situation?


A) Voluntary consent
B) Freedom from harm
C) Protection from discomfort
D) Fair and equitable treatment

Correct Answer

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Women have been excluded as participants in many randomized controlled trials because


A) it is difficult to include both genders.
B) female hormones may interact with the drugs studied.
C) women are generally more difficult to recruit as participants.
D) female participants may not realize they are pregnant, thus putting the fetus at risk.

Correct Answer

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What factors might influence whether it is ethical to require an older adult to participate in a research study?


A) The relevance of the research to issues important to older adults
B) The ethnic background of the potential participant
C) The age of the potential participant
D) The cognitive capacity of the potential participant
E) The degree of risk associated with the study

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You are a staff nurse,and you observe a health care professional coercing a patient to agree to participate in a research study.What should you do in this situation?


A) Contact the hospital's REB.
B) Confront the researcher with your concerns.
C) Document your suspicions in the patient's medical record.
D) Secretly record the researcher's interaction with the patient.

Correct Answer

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Which is considered an essential element of the informed consent form for a research study?


A) The witnessing signature of an authorized party
B) The listing of members of the agency's REB
C) Explanation of whom to contact regarding any area of the study
D) List of participant's assignment to intervention group or control group

Correct Answer

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A staff nurse overhears a health care professional use coercion to make a patient agree to participate in a research study.What should the staff nurse do?


A) Confront the researcher with concerns.
B) Document suspicions in the patient's medical record.
C) Contact the hospital's REB.
D) Secretly record the researcher's interaction with a potential participant.

Correct Answer

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What are ethical principles that are illustrated by obtaining REB approval?


A) Respect
B) Beneficence
C) Trust
D) Justice
E) Anonymity
F) Confidentiality

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Which statements,descriptions,or pieces of information are considered an essential element of the informed consent form for a research study?


A) "Patients who were contacted by study personnel and who signed (or whose proxy signed) informed consent were enrolled in the study cohort."
B) "The research has been reviewed and approved by the Human Participants' Review Committee, which include Jane Doe and John Smith."
C) "If you have any concerns about the conduct of this study or your rights as a research participant, please contact Jay Tee, lead investigator for this project at…"
D) "You have been randomly assigned to the intervention group, which will receive a new experimental drug developed to prevent breast cancer."

Correct Answer

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C

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